rs878853374

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs878853374(C;T)

Make rs878853374(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

38304761

Gene

RPGR

is a	snp
is	mentioned by
dbSNP	rs878853374
dbSNP (classic)	rs878853374
ClinGen	rs878853374
ebi	rs878853374
HLI	rs878853374
Exac	rs878853374
Gnomad	rs878853374
Varsome	rs878853374
LitVar	rs878853374
Map	rs878853374
PheGenI	rs878853374
Biobank	rs878853374
1000 genomes	rs878853374
hgdp	rs878853374
ensembl	rs878853374
geneview	rs878853374
scholar	rs878853374
google	rs878853374
pharmgkb	rs878853374
gwascentral	rs878853374
openSNP	rs878853374
23andMe	rs878853374
SNPshot	rs878853374
SNPdbe	rs878853374
MSV3d	rs878853374
GWAS Ctlg	rs878853374

Max Magnitude

0

ClinVar
Risk	rs878853374(T;T)
Alt	rs878853374(T;T)
Reference	Rs878853374(C;C)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	RPGR
CLNDBN	Retinal dystrophy
Reversed	1
HGVS	NC_000023.10:g.38164014G>A
CLNSRC
CLNACC	RCV000225612.1,